Primary Device ID | 05055272711852 |
NIH Device Record Key | 3b2a0b5d-7044-4b39-abad-a87d8f71b104 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3mm Glaucoma Probe |
Version Model Number | 2509-P-8025 |
Company DUNS | 210164398 |
Company Name | KEELER LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |